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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by LCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 601 | 11 | 14 | 1647 1997 CLINICAL GENETICS 52(4):211-215 Arvio M; Peippo M; Simola KOJ Applicability of a checklist for clinical screening of the fragile X syndrome | 10 | 15 |
| 602 | 7 | 10 | 1682 1997 JOURNAL OF MEDICAL GENETICS 34(3):250-251 Willemsen R; Los F; Mohkamsing S; vandenOuweland A; Deelen W; et al. Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A new appraisal | 10 | 12 |
| 603 | 42 | 92 | 1692 1997 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 3(4):313-322 Abbeduto L; Hagerman RJ Language and communication in fragile X syndrome | 10 | 17 |
| 604 | 17 | 31 | 1700 1997 NUCLEIC ACIDS RESEARCH 25(14):2883-2887 Sandberg G; Schalling M Effect of in vitro promoter methylation and CGG repeat expansion on FMR-1 expression | 10 | 24 |
| 605 | 13 | 26 | 1827 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):257-263 Fisch GS; Carpenter NJ; Holden JJA; Simensen R; Howard-Peebles PN; et al. Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: Growth, development, and profiles | 10 | 10 |
| 606 | 11 | 20 | 1834 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):308-312 Fisch GS; Carpenter N; Holden JJA; Howard-Peebles PN; Maddalena A; et al. Longitudinal changes in cognitive and adaptive behavior in fragile X females: A prospective multicenter analysis | 10 | 16 |
| 607 | 5 | 6 | 1838 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):326-326 Vianna-Morgante AM Twinning and premature ovarian failure in premutation fragile X carriers | 10 | 11 |
| 608 | 5 | 11 | 1839 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):327-328 Braat DDM; Smits APT; Thomas CMG Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: A pilot study | 10 | 13 |
| 609 | 19 | 37 | 1846 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):184-190 Patsalis PC; Sismani C; Hettinger JA; Boumba I; Georgiou I; et al. Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: Incidence, genetic variation, and stability | 10 | 20 |
| 610 | 22 | 54 | 1888 1999 EPILEPSIA 40(8):1092-1099 Musumeci SA; Hagerman RJ; Ferri R; Bosco P; Dalla Bernardina B; et al. Epilepsy and EEG findings in males with fragile X syndrome | 10 | 19 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 611 | 17 | 41 | 2026 2000 HUMAN REPRODUCTION 15(1):197-202 Marozzi A; Vegetti W; Manfredini E; Tibiletti MG; Testa G; et al. Association between idiopathic premature ovarian failure and fragile X premutation | 10 | 30 |
| 612 | 26 | 47 | 2187 2001 NEUROPSYCHOLOGY 15(2):290-299 Bennetto L; Pennington BF; Porter D; Taylor AK; Hagerman RJ Profile of cognitive functioning in women with the fragile X mutation | 10 | 13 |
| 613 | 24 | 62 | 2416 2003 DEVELOPMENT 130(22):5543-5552 Lee A; Li WJ; Xu KY; Bogert BA; Su K; et al. Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1 | 10 | 15 |
| 614 | 7 | 35 | 2464 2003 NEURON 39(5):739-747 Jin P; Zarnescu DC; Zhang FP; Pearson CE; Lucchesi JC; et al. RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila | 10 | 23 |
| 615 | 22 | 39 | 2467 2003 NEUROSCIENCE 120(4):1005-1017 Chen L; Yun SW; Seto J; Liu W; Toth M The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences | 10 | 11 |
| 616 | 36 | 60 | 2477 2003 TRENDS IN GENETICS 19(3):148-154 Kooy RF Of mice and the fragile X syndrome | 10 | 13 |
| 617 | 12 | 37 | 2559 2004 JOURNAL OF NEUROSCIENCE 24(11):2648-2655 Antar LN; Afroz R; Dictenberg JB; Carroll RC; Bassell GJ Metabotropic glutamate receptor activation regulates Fragile X mental retardation protein and Fmr1 mRNA localization differentially in dendrites and at synapses | 10 | 15 |
| 618 | 1 | 10 | 136 1983 CYTOGENETICS AND CELL GENETICS 35(3):223-225 BRYANT EM; MARTIN GM; HOEHN H FRAGILE-X EXPRESSION STUDIED BY CLONAL ANALYSIS AND SOMATIC-CELL HYBRIDIZATION | 9 | 12 |
| 619 | 1 | 12 | 174 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):123-131 HAGERMAN RJ; SYNHORST DP MITRAL-VALVE PROLAPSE AND AORTIC DILATATION IN THE FRAGILE-X SYNDROME | 9 | 17 |
| 620 | 32 | 83 | 218 1984 JOURNAL OF MEDICAL GENETICS 21(2):84-91 DEARCE MA; KEARNS A THE FRAGILE X-SYNDROME - THE PATIENTS AND THEIR CHROMOSOMES | 9 | 20 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 621 | 0 | 0 | 220 1984 JOURNAL OF MEDICAL GENETICS 21(4):299-299 PEMBREY ME; WINTER RM; DAVIES KE A PERMUTATION THAT GENERATES THE DEFINITIVE MUTATION BY RECOMBINATION EXPLAINS THE INHERITANCE OF THE MARTIN-BELL SYNDROME (FRAGILE-X) | 9 | 13 |
| 622 | 11 | 29 | 244 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(3):543-552 ROSENBLATT DS; DUSCHENES EA; HELLSTROM FV; GOLICK MS; VEKEMANS MJJ; et al. FOLIC-ACID BLINDED TRIAL IN IDENTICAL-TWINS WITH FRAGILE-X SYNDROME | 9 | 13 |
| 623 | 9 | 17 | 330 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):263-271 BROWN WT; COHEN IL; FISCH GS; WOLFSCHEIN EG; JENKINS VA; et al. HIGH-DOSE FOLIC-ACID TREATMENT OF FRAGILE-(X) MALES | 9 | 14 |
| 624 | 9 | 31 | 362 1986 ANNALS OF HUMAN GENETICS 50:385-398 LOESCH DZ DERMATOGLYPHIC FINDINGS IN FRAGILE X-SYNDROME - A CAUSAL HYPOTHESIS POINTS TO X-Y INTERCHANGE | 9 | 14 |
| 625 | 0 | 18 | 376 1986 CLINICAL ENDOCRINOLOGY 24(3):327-333 OHARE JP; OBRIEN IAD; ARENDT J; ASTLEY P; RATCLIFFE W; et al. DOES MELATONIN DEFICIENCY CAUSE THE ENLARGED GENITALIA OF THE FRAGILE-X SYNDROME | 9 | 11 |
| 626 | 2 | 7 | 378 1986 CLINICAL GENETICS 29(3):191-195 HECHT F; FRYNS JP; VLIETINCK RF; VANDENBERGHE H GENETIC-CONTROL OVER FRAGILE X-CHROMOSOME EXPRESSION | 9 | 10 |
| 627 | 3 | 15 | 389 1986 HUMAN GENETICS 73(1):20-22 ABRUZZO MA; PETTAY D; MAYER M; JACOBS PA THE EFFECT OF CAFFEINE ON FRAGILE-X EXPRESSION | 9 | 12 |
| 628 | 5 | 36 | 415 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(2):184-187 HAGERMAN RJ; ALTSHULSTARK D; MCBOGG P RECURRENT OTITIS-MEDIA IN THE FRAGILE X-SYNDROME | 9 | 14 |
| 629 | 16 | 30 | 459 1987 HUMAN GENETICS 76(2):165-172 BUCHANAN JA; BUCKTON KE; GOSDEN CM; NEWTON MS; CLAYTON JF; et al. 10 FAMILIES WITH FRAGILE-X SYNDROME - LINKAGE RELATIONSHIPS WITH 4 DNA PROBES FROM DISTAL-XQ | 9 | 16 |
| 630 | 12 | 22 | 496 1987 PRENATAL DIAGNOSIS 7(3):203-214 WEBB TP; RODECK CH; NICOLAIDES KH; GOSDEN CM PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME USING FETAL BLOOD AND AMNIOTIC-FLUID | 9 | 18 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 631 | 4 | 16 | 516 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):99-107 FILIPPI G; PECILE V; RINALDI A; SINISCALCO M FRAGILE-X MUTATION AND KLINEFELTER SYNDROME - A REAPPRAISAL | 9 | 13 |
| 632 | 16 | 24 | 594 1988 HUMAN GENETICS 80(4):375-378 VOELCKEL MA; MATTEI MG; NGUYEN C; PHILIP N; BIRG F; et al. DISSOCIATION BETWEEN MENTAL-RETARDATION AND FRAGILE SITE EXPRESSION IN A FAMILY WITH FRAGILE X-LINKED MENTAL-RETARDATION | 9 | 16 |
| 633 | 3 | 13 | 604 1988 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 29(4):447-451 GILLBERG C; OHLSON VA; WAHLSTROM J; STEFFENBURG S; BLIX K MONOZYGOTIC FEMALE TWINS WITH AUTISM AND THE FRAGILE-X SYNDROME (AFRAX) | 9 | 19 |
| 634 | 6 | 24 | 679 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):181-187 MACKINNON RN; HIRST MC; BELL MV; WATSON JEV; CLAUSSEN U; et al. MICRODISSECTION OF THE FRAGILE-X REGION | 9 | 37 |
| 635 | 18 | 35 | 865 1991 GENOMICS 10(3):576-582 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; et al. LINKAGE HOMOGENEITY NEAR THE FRAGILE-X LOCUS IN NORMAL AND FRAGILE-X FAMILIES | 9 | 13 |
| 636 | 16 | 19 | 954 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):333-338 GABARRON J; LOPEZ I; GLOVER G; CARBONELL P FRAGILE-X SCREENING-PROGRAM IN A SPANISH REGION | 9 | 10 |
| 637 | 1 | 3 | 1141 1993 LANCET 341(8847):770-770 HOWARDPEEBLES PN; MADDALENA A; BLACK SH; SCHULMAN JD POPULATION SCREENING FOR FRAGILE-X SYNDROME | 9 | 10 |
| 638 | 3 | 25 | 1152 1993 NATURE GENETICS 3(1):44-48 HANZLIK AJ; OSEMLAKHANZLIK MM; HAUSER MA; KURNIT DM A RECOMBINATION-BASED ASSAY DEMONSTRATES THAT THE FRAGILE-X SEQUENCE IS TRANSCRIBED WIDELY DURING DEVELOPMENT | 9 | 14 |
| 639 | 7 | 13 | 1179 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):339-345 FISCH GS; NELSON DL; SNOW K; THIBODEAU SN; CHALIFOUX M; et al. RELIABILITY OF DIAGNOSTIC-ASSESSMENT OF NORMAL AND PREMUTATION STATUS IN THE FRAGILE-X-SYNDROME USING DNA TESTING | 9 | 11 |
| 640 | 9 | 16 | 1181 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):353-357 FISCH GS; SIMENSEN R; ARINAMI T; BORGHGRAEF M; FRYNS JP LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X FEMALES - A PRELIMINARY MULTICENTER ANALYSIS | 9 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 641 | 18 | 33 | 1211 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):517-521 CHIURAZZI P; KOZAK L; NERI G UNSTABLE TRIPLETS AND THEIR MUTATIONAL MECHANISM - SIZE-REDUCTION OF THE CGG REPEAT VS GERMLINE MOSAICISM IN THE FRAGILE-X-SYNDROME | 9 | 15 |
| 642 | 10 | 23 | 1254 1994 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 24(4):473-485 MAZZOCCO MMM; PENNINGTON BF; HAGERMAN RJ SOCIAL COGNITION SKILLS AMONG FEMALES WITH FRAGILE-X | 9 | 12 |
| 643 | 12 | 21 | 1321 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(5):991-993 SHERMAN SL THE HIGH PREVALENCE OF FRAGILE-X PREMUTATION CARRIER FEMALES - IS THIS FREQUENCY UNIQUE TO THE FRENCH-CANADIAN POPULATION | 9 | 14 |
| 644 | 18 | 31 | 1397 1995 HUMAN MOLECULAR GENETICS 4(9):1681-1684 QUAN F; GROMPE M; JAKOBS P; POPOVICH BW SPONTANEOUS DELETION IN THE FMR1 GENE IN A PATIENT WITH FRAGILE-X SYNDROME AND CHERUBISM | 9 | 14 |
| 645 | 14 | 20 | 1441 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(1):237-239 Antinolo G; Borrego S; Cabeza JC; Sanchez R; Sanchez J; et al. Reverse mutation in fragile X syndrome | 9 | 11 |
| 646 | 4 | 11 | 1462 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):198-202 Robinson H; Wake S; Wright F; Laing S; Turner G Informed choice in fragile X syndrome and its effects on prevalence | 9 | 11 |
| 647 | 14 | 20 | 1467 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):234-238 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; et al. Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus | 9 | 15 |
| 648 | 12 | 21 | 1475 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):278-282 Lachiewicz AM; Spiridigliozzi GA; McConkieRosell A; Burgess D; Feng Y; et al. A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene | 9 | 11 |
| 649 | 16 | 20 | 1477 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):293-295 Mannermaa A; Pulkkinen L; Kajanoja E; Ryynanen M; Saarikoski S Deletion in the FMR1 gene in a fragile-X male | 9 | 9 |
| 650 | 17 | 24 | 1478 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):296-301 Dobkin CS; Nolin SL; Cohen I; Sudhalter V; Bialer MG; et al. Tissue differences in fragile X mosaics: Mosaicism in blood cells may differ greatly from skin | 9 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 651 | 15 | 26 | 1536 1996 HUMAN GENETICS 97(6):808-812 Haddad LA; MingroniNetto RC; ViannaMorgante AM; Pena SDJ A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males | 9 | 16 |
| 652 | 19 | 36 | 1756 1998 HUMAN REPRODUCTION 13(5):1184-1187 Conway GS; Payne NN; Webb J; Murray A; Jacobs PA Fragile X premutation screening in women with premature ovarian failure | 9 | 33 |
| 653 | 13 | 65 | 1886 1999 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 41(9):625-632 Hatton DD; Bailey DB; Hargett-Beck MQ; Skinner M; Clark RD Behavioral style of young boys with fragile X syndrome | 9 | 13 |
| 654 | 18 | 33 | 1890 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(5):526-532 Kooy RF; Reyniers E; Verhoye M; Sijbers J; Bakker CE; et al. Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging | 9 | 21 |
| 655 | 27 | 67 | 1900 1999 HUMAN MOLECULAR GENETICS 8(12):2293-2302 Burman RW; Popovich BW; Jacky PB; Turker MS Fully expanded FMR1 CGG repeats exhibit a length-and differentiation-dependent instability in cell hybrids that is independent of DNA methylation | 9 | 12 |
| 656 | 8 | 10 | 1910 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:47-53 Carmichael B; Pembrey M; Turner G; Barnicoat A Diagnosis of fragile-X syndrome: the experiences of parents | 9 | 11 |
| 657 | 32 | 52 | 1937 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):480-493 Crawford DC; Schwartz CE; Meadows KL; Newman JL; Taft LF; et al. Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population | 9 | 18 |
| 658 | 2 | 4 | 1939 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):253-254 Murray A; Ennis S; Morton N No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers | 9 | 17 |
| 659 | 11 | 59 | 1994 2000 CELL 100(3):323-332 Lewis HA; Musunuru K; Jensen KB; Edo C; Chen H; et al. Sequence-specific RNA binding by a Nova KH domain: Implications for paraneoplastic disease and the fragile X syndrome | 9 | 97 |
| 660 | 26 | 55 | 2021 2000 HUMAN MOLECULAR GENETICS 9(10):1487-1493 Tamanini F; Kirkpatrick LL; Schonkeren J; van Unen L; Bontekoe C; et al. The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins | 9 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 661 | 13 | 39 | 2038 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(4):278-282 Wisbeck JM; Huffman LC; Freund L; Gunnar MR; Davis EP; et al. Cortisol and social stressors in children with fragile X: A pilot study | 9 | 11 |
| 662 | 13 | 43 | 2122 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):28-38 Belser RC; Sudhalter V Conversational characteristics of children with fragile X syndrome: Repetitive speech | 9 | 12 |
| 663 | 34 | 53 | 2130 2001 BRAIN 124:1610-1618 Eliez S; Blasey CM; Freund LS; Hastie T; Reiss AL Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome | 9 | 15 |
| 664 | 1 | 4 | 2426 2003 HUMAN GENETICS 112(5-6):619-620 Macpherson J; Waghorn A; Hammans S; Jacobs P Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia | 9 | 18 |
| 665 | 1 | 7 | 33 1981 NEW ENGLAND JOURNAL OF MEDICINE 305(22):1348-1348 NIELSEN KB; TOMMERUP N; DYGGVE H; SCHOU C MACROORCHIDISM, MENTAL-RETARDATION, AND THE FRAGILE-X | 8 | 12 |
| 666 | 8 | 46 | 70 1982 JOHNS HOPKINS MEDICAL JOURNAL 151(5):231-237 PYERITZ RE; STAMBERG J; THOMAS GH; BELL BB; ZAHKA KG; et al. THE MARKER XQ28 SYNDROME (FRAGILE-X SYNDROME) IN A RETARDED MAN WITH MITRAL-VALVE PROLAPSE | 8 | 13 |
| 667 | 5 | 26 | 90 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(5):869-878 POPOVICH BW; ROSENBLATT DS; COOPER BA; VEKEMANS M INTRACELLULAR FOLATE DISTRIBUTION IN CULTURED FIBROBLASTS FROM PATIENTS WITH THE FRAGILE-X SYNDROME | 8 | 12 |
| 668 | 8 | 23 | 129 1983 CLINICAL GENETICS 23(6):436-440 SILVERMAN W; LUBIN R; JENKINS EC; BROWN WT THE STRENGTH OF ASSOCIATION BETWEEN FRAGILE(X) CHROMOSOME PRESENCE AND MENTAL-RETARDATION | 8 | 11 |
| 669 | 0 | 4 | 170 1984 AMERICAN JOURNAL OF HUMAN GENETICS 36(1):227-229 MIEZEJESKI CM; JENKINS EC; HILL AL; WISNIEWSKI K; BROWN WT VERBAL VS NONVERBAL ABILITY, FRAGILE-X SYNDROME, AND HETEROZYGOUS CARRIERS | 8 | 9 |
| 670 | 4 | 11 | 192 1984 ANNALES DE GENETIQUE 27(4):230-232 LEJEUNE J; RETHORE MO; DEBLOIS MC; RAVEL A ASSAY OF FOLIC-ACID TREATMENT IN FRAGILE-X SYNDROME | 8 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 671 | 2 | 17 | 289 1985 HUMAN GENETICS 69(4):327-331 MATTEI MG; BAETEMAN MA; HEILIG R; OBERLE I; DAVIES K; et al. LOCALIZATION BY INSITU HYBRIDIZATION OF THE COAGULATION FACTOR-IX GENE AND OF 2 POLYMORPHIC DNA PROBES WITH RESPECT TO THE FRAGILE-X SITE | 8 | 49 |
| 672 | 7 | 33 | 458 1987 HUMAN GENETICS 76(2):141-147 JOHANNISSON R; REHDER H; WENDT V; SCHWINGER E SPERMATOGENESIS IN 2 PATIENTS WITH THE FRAGILE-X SYNDROME .1. HISTOLOGY - LIGHT AND ELECTRON-MICROSCOPY | 8 | 15 |
| 673 | 4 | 11 | 463 1987 HUMAN GENETICS 77(1):92-94 ARINAMI T; KONDO I; HAMAGUCHI H; TAMURA K; HIRANO T A FRAGILE-X FEMALE WITH DOWN-SYNDROME | 8 | 11 |
| 674 | 10 | 24 | 501 1988 AMERICAN JOURNAL OF HUMAN GENETICS 43(1):46-51 ARINAMI T; SATO M; NAKAJIMA S; KONDO I AUDITORY BRAIN-STEM RESPONSES IN THE FRAGILE-X SYNDROME | 8 | 11 |
| 675 | 22 | 61 | 531 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):355-368 MCKINLEY MJ; KEARNEY LU; NICOLAIDES KH; GOSDEN CM; WEBB TP; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME BY PLACENTAL (CHORIONIC VILLI) BIOPSY CULTURE | 8 | 13 |
| 676 | 12 | 22 | 544 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):551-566 BROWN WT; YE W; GROSS AC; CHAN CB; DOBKIN CS; et al. MULTIPOINT LINKAGE OF 9 ANONYMOUS PROBES TO HPRT, FACTOR-IX, AND FRAGILE-X | 8 | 25 |
| 677 | 4 | 30 | 591 1988 HUMAN GENETICS 79(4):292-296 LI SY; TSAI CC; CHOU MY; LIN JK A CYTOGENETIC STUDY OF MENTALLY-RETARDED SCHOOL-CHILDREN IN TAIWAN WITH SPECIAL REFERENCE TO THE FRAGILE X-CHROMOSOME | 8 | 18 |
| 678 | 2 | 6 | 602 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):458-460 LECOUTEUR A; RUTTER M; SUMMERS D; BUTLER L FRAGILE-X IN FEMALE AUTISTIC TWINS | 8 | 14 |
| 679 | 9 | 21 | 711 1990 HUMAN GENETICS 85(6):590-594 YU WD; WENGER SL; STEELE MW X-CHROMOSOME IMPRINTING IN FRAGILE-X SYNDROME | 8 | 16 |
| 680 | 11 | 25 | 811 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):391-395 LAIRD CD POSSIBLE ERASURE OF THE IMPRINT ON A FRAGILE-X CHROMOSOME WHEN TRANSMITTED BY A MALE | 8 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 681 | 11 | 29 | 925 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):111-115 GRIGSBY J; KEMPER MB; HAGERMAN RJ VERBAL-LEARNING AND MEMORY AMONG HETEROZYGOUS FRAGILE-X FEMALES | 8 | 8 |
| 682 | 5 | 25 | 962 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(5):543-550 LOESCH DZ; HAY DA; SHEFFIELD LJ FRAGILE-X FAMILY WITH UNUSUAL DIGITAL AND FACIAL ABNORMALITIES, CLEFT-LIP AND PALATE, AND EPILEPSY | 8 | 12 |
| 683 | 7 | 7 | 1093 1993 CLINICAL GENETICS 43(3):157-159 MORNET E; JOKIC M; BOGYO A; TEJADA I; DELUCHAT C; et al. AFFECTED SIBS WITH FRAGILE-X SYNDROME EXHIBIT AN AGE-DEPENDENT DECREASE IN THE SIZE OF THE FRAGILE-X FULL MUTATION | 8 | 8 |
| 684 | 3 | 4 | 1142 1993 LANCET 341(8847):770-770 BUNDEY S; NORMAN E POPULATION SCREENING FOR FRAGILE-X SYNDROME | 8 | 8 |
| 685 | 8 | 10 | 1205 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):486-489 VONKOSKULL H; GAHMBERG N; SALONEN R; SALO A; PEIPPO M FRAXA LOCUS IN FRAGILE-X DIAGNOSIS - FAMILY STUDIES, PRENATAL-DIAGNOSIS, AND DIAGNOSIS OF SPORADIC CASES OF MENTAL-RETARDATION | 8 | 8 |
| 686 | 58 | 91 | 1233 1994 EUROPEAN JOURNAL OF CLINICAL INVESTIGATION 24(1):1-10 ROUSSEAU F THE FRAGILE-X SYNDROME - IMPLICATIONS OF MOLECULAR-GENETICS FOR THE CLINICAL SYNDROME | 8 | 11 |
| 687 | 21 | 27 | 1323 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1408-1413 LOESCH DZ; HUGGINS R; PETROVIC V; SLATER H EXPANSION OF THE CGG REPEAT IN FRAGILE-X IN THE FMR1 GENE DEPENDS ON THE SEX OF THE OFFSPRING | 8 | 13 |
| 688 | 26 | 39 | 1347 1995 BRAIN & DEVELOPMENT 17(5):317-321 NANBA E; KOHNO Y; MATSUDA A; YANO M; SATO C; et al. NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED JAPANESE MALES | 8 | 17 |
| 689 | 71 | 117 | 1433 1995 PEDIATRIC RESEARCH 38(5):629-637 OOSTRA BA; HALLEY DJJ COMPLEX BEHAVIOR OF SIMPLE REPEATS - THE FRAGILE-X SYNDROME | 8 | 11 |
| 690 | 14 | 24 | 1483 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):329-333 AllinghamHawkins DJ; Brown CA; Babul R; Chitayat D; Krekewich K; et al. Tissue-specific methylation differences and cognitive function in fragile X premutation females | 8 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 691 | 9 | 15 | 1646 1997 CLINICAL GENETICS 52(3):147-154 Hecimovic S; Barisic I; Muller A; Petkovic I; Baric I; et al. Expand long PCR for fragile X mutation detection | 8 | 23 |
| 692 | 15 | 19 | 1662 1997 HUMAN GENETICS 100(5-6):564-568 Larsen LA; Gronskov K; NorgaardPedersen B; BrondumNielsen K; Hasholt L; et al. High-throughput analysis of fragile X (CGG)(n) alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis | 8 | 24 |
| 693 | 24 | 69 | 1703 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(9):4587-4592 Hansen RS; Canfield TK; Fjeld AD; Mumm S; Laird CD; et al. A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication | 8 | 41 |
| 694 | 12 | 30 | 1723 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):18-23 Guerreiro MM; Camargo EE; Kato M; Marques-De-Faria AP; Ciasca SM; et al. Fragile X syndrome - Clinical, electroencephalographic and neuroimaging characteristics | 8 | 14 |
| 695 | 10 | 40 | 1781 1998 JOURNAL OF MOLECULAR BIOLOGY 275(1):3-16 Darlow JM; Leach DRF Secondary structures in d(CGG) and d(CCG) repeat tracts | 8 | 44 |
| 696 | 27 | 52 | 1800 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(3):680-688 Nolin SL; Houck GE; Gargano AD; Blumstein H; Dobkin CS; et al. FMR1 CCG-repeat instability by single sperm and lymphocytes of fragile-X premutation males | 8 | 15 |
| 697 | 27 | 53 | 1821 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(1):25-30 Abrams MT; Kaufmann WE; Rousseau F; Oostra BA; Wolozin B; et al. FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome | 8 | 11 |
| 698 | 18 | 31 | 1845 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):179-183 Pang CP; Poon PMK; Chen QL; Lai KYC; Yin CH; et al. Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients | 8 | 11 |
| 699 | 20 | 43 | 1922 1999 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 38(10):1294-1301 Murphy DGM; Mentis MJ; Pietrini P; Grady CL; Moore CJ; et al. Premutation female carriers of fragile X syndrome: A pilot study on brain anatomy and metabolism | 8 | 9 |
| 700 | 6 | 8 | 1940 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):254-255 Vianna-Morgante AM; Costa SS Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X | 8 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 701 | 30 | 59 | 1974 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):150-156 Backes M; Genc B; Schreck J; Doerfler W; Lehmkuhl G; et al. Cognitive and behavioral profile of fragile X boys: Correlations to molecular data | 8 | 12 |
| 702 | 2 | 29 | 1987 2000 BEHAVIOR RESEARCH METHODS INSTRUMENTS & COMPUTERS 32(1):5-10 Boccia ML; Roberts JE Behavior and autonomic nervous system function assessed via heart period measures: The case of hyperarousal in boys with fragile X syndrome | 8 | 11 |
| 703 | 11 | 52 | 1992 2000 BRAIN AND COGNITION 44(3):387-401 Munir F; Cornish KM; Wilding J Nature of the working memory deficit in Fragile-X syndrome | 8 | 9 |
| 704 | 12 | 16 | 2063 2000 JOURNAL OF MEDICAL GENETICS 37(8):603-604 Willemsen R; Olmer R; Otero YD; Oostra BA Twin sisters, monozygotic with the fragile X mutation, but with a different phenotype | 8 | 8 |
| 705 | 27 | 39 | 2117 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(4):314-319 Johnston C; Eliez S; Dyer-Friedman J; Hessl D; Glaser B; et al. Neurobehavioral phenotype in carriers of the fragile X premutation | 8 | 9 |
| 706 | 37 | 73 | 2140 2001 COGNITIVE NEUROPSYCHOLOGY 18(1):1-18 Simon JA; Keenan JM; Pennington BF; Taylor AK; Hagerman RJ Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence | 8 | 10 |
| 707 | 7 | 25 | 2160 2001 HUMAN REPRODUCTION 16(3):457-462 Hundscheid RDL; Braat DDM; Kiemeney LALM; Smits APT; Thomas CMG Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives | 8 | 13 |
| 708 | 33 | 52 | 2316 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):179-186 Keysor CS; Mazzocco MMM A developmental approach to understanding fragile X syndrome in females | 8 | 9 |
| 709 | 39 | 53 | 2429 2003 HUMAN MOLECULAR GENETICS 12(14):1689-1698 Bardoni B; Castets M; Huot ME; Schenck A; Adinolfi S; et al. 82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization | 8 | 8 |
| 710 | 30 | 56 | 2437 2003 JOURNAL OF BIOLOGICAL CHEMISTRY 278(18):15669-15678 Sung YJ; Dolzhanskaya N; Nolin SL; Brown T; Currie JR; et al. The fragile X mental retardation protein FMRP binds elongation factor 1A mRNA and negatively regulates its translation in vivo | 8 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 711 | 22 | 45 | 2473 2003 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 100(24):14374-14378 Todd PK; Mack KJ; Malter JS The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95 | 8 | 13 |
| 712 | 41 | 80 | 2480 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):805-816 Hagerman PJ; Hagerman RJ The fragile-X premutation: A maturing perspective | 8 | 14 |
| 713 | 33 | 95 | 2619 2004 TRENDS IN NEUROSCIENCES 27(7):370-377 Bear MF; Huber KM; Warren ST The mGIuR theory of fragile X mental retardation | 8 | 10 |
| 714 | 0 | 24 | 8 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(5):752-761 MARENI C; MIGEON BR FRAGILE-X SYNDROME - SEARCH FOR PHENOTYPIC MANIFESTATIONS AT LOCI FOR HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE AND GLUCOSE-6-PHOSPHATE-DEHYDROGENASE | 7 | 10 |
| 715 | 2 | 7 | 65 1982 HUMAN GENETICS 61(2):163-164 EBERLE G; ZANKL H; ZANKL M CO-CULTIVATION STUDIES WITH CELLS OF PATIENTS BEARING FRAGILE-X CHROMOSOMES | 7 | 11 |
| 716 | 2 | 11 | 222 1984 JOURNAL OF NERVOUS AND MENTAL DISEASE 172(9):549-551 KERBESHIAN J; BURD L; MARTSOLF J A FAMILY WITH FRAGILE-X SYNDROME | 7 | 20 |
| 717 | 3 | 11 | 230 1984 OBSTETRICS AND GYNECOLOGY 63(3):S19-S21 HOGGE WA; SCHONBERG SA; GLOVER TW; HECHT F; GOLBUS MS PRENATAL-DIAGNOSIS OF FRAGILE (X) SYNDROME | 7 | 14 |
| 718 | 21 | 26 | 334 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):313-324 TOMMERUP N; AULA P; GUSTAVII B; HEIBERG A; HOLMGREN G; et al. 2ND TRIMESTER PRENATAL-DIAGNOSIS OF THE FRAGILE-X | 7 | 14 |
| 719 | 7 | 12 | 381 1986 CLINICAL GENETICS 30(4):249-254 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; et al. ANALYSIS OF FRAGILE X-MENTAL RETARDATION FAMILIES USING FLANKING POLYMORPHIC DNA PROBES | 7 | 13 |
| 720 | 9 | 16 | 398 1986 JOURNAL OF MEDICAL GENETICS 23(5):400-406 WEBB T; THAKE A; TODD J 12 FAMILIES WITH FRAGILE X(Q27) | 7 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 721 | 24 | 48 | 414 1986 TRENDS IN NEUROSCIENCES 9(2):58-62 PEMBREY ME; WINTER RM; DAVIES KE FRAGILE X MENTAL-RETARDATION - CURRENT CONTROVERSIES | 7 | 9 |
| 722 | 17 | 36 | 427 1987 ANNALS OF HUMAN GENETICS 51:107-124 GIANNELLI F; MORRIS AH; GARRETT C; DAKER M; THURSTON C; et al. GENETIC-HETEROGENEITY OF X-LINKED MENTAL-RETARDATION WITH FRAGILE-X - ASSOCIATION OF TIGHT LINKAGE TO FACTOR-IX AND INCOMPLETE PENETRANCE IN MALES | 7 | 16 |
| 723 | 14 | 26 | 460 1987 HUMAN GENETICS 76(4):344-347 ARINAMI T; KONDO I; NAKAJIMA S; HAMAGUCHI H FREQUENCY OF THE FRAGILE X-SYNDROME IN INSTITUTIONALIZED MENTALLY-RETARDED FEMALES IN JAPAN | 7 | 9 |
| 724 | 16 | 41 | 472 1987 JOURNAL OF MEDICAL GENETICS 24(1):14-22 CONNOR JM; PIRRIT LA; YATES JRW; CROSSLEY JA; IMRIE SJ; et al. LINKAGE ANALYSIS USING MULTIPLE XQ DNA POLYMORPHISMS IN NORMAL-FAMILIES, FAMILIES WITH THE FRAGILE X-SYNDROME, AND OTHER FAMILIES WITH X-LINKED CONDITIONS | 7 | 12 |
| 725 | 4 | 18 | 480 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:73-79 PUESCHEL SM; OBRIEN MM; PADREMENDOZA T KLINEFELTER SYNDROME AND ASSOCIATED FRAGILE-X SYNDROME | 7 | 8 |
| 726 | 0 | 18 | 514 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):77-82 PHELAN MC; STEVENSON RE; COLLINS JL; TRENT HE FRAGILE-X SYNDROME AND NEOPLASIA | 7 | 13 |
| 727 | 3 | 8 | 535 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):401-406 FRYNS JP; VANDENBERGHE H INACTIVATION PATTERN OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 7 | 11 |
| 728 | 4 | 18 | 546 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):613-623 WARREN ST; ZHANG F; SUTCLIFFE JS; PETERS JF STRATEGY FOR MOLECULAR-CLONING OF THE FRAGILE-X SITE DNA | 7 | 12 |
| 729 | 2 | 5 | 554 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):693-696 LAIRD CD FRAGILE-X MUTATION PROPOSED TO BLOCK COMPLETE REACTIVATION IN FEMALES OF AN INACTIVE X-CHROMOSOME | 7 | 10 |
| 730 | 8 | 13 | 558 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):735-739 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; et al. MARTIN-BELL SYNDROME IN GREECE, WITH REPORT OF ANOTHER 47,XXY FRAGILE X PATIENT | 7 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 731 | 6 | 7 | 650 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(3):473-476 BOLTON P; RUTTER M; BUTLER L; SUMMERS D FEMALES WITH AUTISM AND THE FRAGILE-X | 7 | 11 |
| 732 | 6 | 44 | 708 1990 HUMAN GENETICS 84(4):347-352 SCHMIDT M; CERTOMA A; DUSART D; KALITSIS P; LEVERSHA M; et al. UNUSUAL X-CHROMOSOME INACTIVATION IN A MENTALLY-RETARDED GIRL WITH AN INTERSTITIAL DELETION XQ27 - IMPLICATIONS FOR THE FRAGILE X-SYNDROME | 7 | 27 |
| 733 | 24 | 65 | 712 1990 HUMAN GENETICS 85(6):659-665 WOHRLE D; FRYNS JP; STEINBACH P FRAGILE-X EXPRESSION AND FRAGILE-X INACTIVATION .1. THE EXPRESSION OF THE FRAGILE SITE AT XQ27.3 IS NOT SUPPRESSED ON INACTIVE X-CHROMOSOMES SEPARATED FROM THE ACTIVE HOMOLOG | 7 | 9 |
| 734 | 10 | 28 | 820 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):440-444 KUPKE KG; SORENG AL; MULLER U ORIGIN OF THE SUPERNUMERARY X-CHROMOSOME IN A PATIENT WITH FRAGILE-X AND KLINEFELTER SYNDROME | 7 | 9 |
| 735 | 6 | 20 | 826 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):488-492 DEVONFLINDT R; BYBEL B; CHUDLEY AE; LOPES F SHORT-TERM-MEMORY AND COGNITIVE VARIABILITY IN ADULT FRAGILE-X FEMALES | 7 | 9 |
| 736 | 24 | 53 | 883 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):825-830 PIVEN J; GAYLE J; LANDA R; WZOREK M; FOLSTEIN S THE PREVALENCE OF FRAGILE-X IN A SAMPLE OF AUTISTIC INDIVIDUALS DIAGNOSED USING A STANDARDIZED INTERVIEW | 7 | 26 |
| 737 | 12 | 37 | 902 1991 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 88(19):8302-8306 POUSTKA A; DIETRICH A; LANGENSTEIN G; TONIOLO D; WARREN ST; et al. PHYSICAL MAP OF HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION | 7 | 75 |
| 738 | 5 | 29 | 910 1992 AMERICAN JOURNAL OF HUMAN GENETICS 50(5):1067-1076 LOESCH DZ; HUGGINS RM FIXED AND RANDOM EFFECTS IN THE VARIATION OF THE FINGER RIDGE COUNT - A STUDY OF FRAGILE-X FAMILIES | 7 | 8 |
| 739 | 10 | 17 | 938 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):187-191 VERKERK AJMH; EUSSEN BHJ; VANHEMEL JO; OOSTRA BA LIMITED SIZE OF THE FRAGILE-X SITE SHOWN BY FLUORESCENCE INSITU HYBRIDIZATION | 7 | 7 |
| 740 | 12 | 15 | 947 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):282-290 TEJADA I; MORNET E; BIANCALANA V; OBERLE I; BOUE J; et al. DIRECT DNA ANALYSIS OF FRAGILE-X SYNDROME IN SPANISH PEDIGREES | 7 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 741 | 25 | 46 | 949 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):299-306 CLARKE A; BRADLEY D; GILLESPIE K; REES D; HOLLAND A; et al. FRAGILE-X MENTAL-RETARDATION AND THE IDURONATE SULFATASE LOCUS - TESTING LAIRD MODEL OF FRA(X) INHERITANCE | 7 | 12 |
| 742 | 4 | 6 | 953 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):328-332 NOLIN SL; SNIDER DA; JENKINS EC; DOBKIN CS; PATCHELL K; et al. NEW-YORK-STATE SCREENING-PROGRAM FOR FRAGILE-X SYNDROME - A PROGRESS REPORT | 7 | 8 |
| 743 | 3 | 3 | 956 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):353-354 DRUGGE U; HOLMGREN G; SONBLOMQUIST HK; DAHL N; GUSTAVSON KH; et al. STUDY OF INDIVIDUALS POSSIBLY AFFECTED WITH THE FRAGILE-X SYNDROME IN A LARGE SWEDISH FAMILY IN THE 18TH TO 20TH CENTURIES | 7 | 7 |
| 744 | 7 | 11 | 959 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(5):905-912 MACPHERSON J; HARVEY J; CURTIS G; WEBB T; HEITZ D; et al. A REINVESTIGATION OF 33 FRAGILE(X) FAMILIES USING PROBE STB12.3 | 7 | 9 |
| 745 | 11 | 16 | 1015 1992 NATURE GENETICS 1(3):157-158 HAGERMAN R CLINICAL CONUNDRUMS IN FRAGILE-X SYNDROME | 7 | 8 |
| 746 | 6 | 26 | 1076 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(4):415-422 LOESCH DZ; HUGGINS RM; CHIN WF EFFECT OF FRAGILE-X ON PHYSICAL AND INTELLECTUAL TRAITS ESTIMATED BY PEDIGREE ANALYSIS | 7 | 9 |
| 747 | 35 | 45 | 1113 1993 HUMAN GENETICS 92(5):491-498 STEINBACH P; WOHRLE D; TARIVERDIAN G; KENNERKNECHT I; BARBI G; et al. MOLECULAR ANALYSIS OF MUTATIONS IN THE GENE FMR-1 SEGREGATING IN FRAGILE X-FAMILIES | 7 | 11 |
| 748 | 17 | 32 | 1175 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):309-314 CHIURAZZI P; DEGRAAFF E; NG J; VERKERK AJMH; WOLFSON S; et al. NO APPARENT INVOLVEMENT OF THE FMR1 GENE IN 5 PATIENTS WITH PHENOTYPIC MANIFESTATIONS OF THE FRAGILE-X-SYNDROME | 7 | 11 |
| 749 | 17 | 18 | 1206 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):490-496 MADDALENA A; HICKS BD; SPENCE WC; LEVINSON G; HOWARDPEEBLES PN PRENATAL-DIAGNOSIS IN KNOWN FRAGILE-X CARRIERS | 7 | 12 |
| 750 | 7 | 41 | 1277 1994 NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY 24(6):413-426 FERRI R; MUSUMECI SA; ELIA M; DELGRACCO S; SCUDERI C; et al. BIT-MAPPED SOMATOSENSORY-EVOKED POTENTIALS IN THE FRAGILE-X SYNDROME | 7 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 751 | 14 | 21 | 1328 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):426-430 MCCONKIEROSELL A; ROBINSON H; WAKE S; STALEY LW; HELLER K; et al. DISSEMINATION OF GENETIC RISK INFORMATION TO RELATIVES IN THE FRAGILE-X SYNDROME - GUIDELINES FOR GENETIC COUNSELORS | 7 | 8 |
| 752 | 9 | 28 | 1330 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(1):39-43 SPINELLI M; ROCHA ACD; GIACHETI CM; RICHIERICOSTA A WORD-FINDING DIFFICULTIES, VERBAL PARAPHASIAS, AND VERBAL DYSPRAXIA IN 10 INDIVIDUALS WITH FRAGILE-X-SYNDROME | 7 | 7 |
| 753 | 6 | 13 | 1442 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(3):641-643 Brown WT; Zhong N; Dobkin C Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution | 7 | 12 |
| 754 | 40 | 74 | 1523 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:679-687 Eberhart DE; Warren ST The molecular basis of fragile X syndrome | 7 | 8 |
| 755 | 19 | 35 | 1576 1996 SOMATIC CELL AND MOLECULAR GENETICS 22(6):435-441 Eberhart DE; Warren ST Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus | 7 | 15 |
| 756 | 8 | 29 | 1621 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(1):62-69 McConkieRosell A; Spiridigliozzi GA; Iafolla T; Tarleton J; Lachiewicz AM Carrier testing in the fragile X syndrome: Attitudes and opinions of obligate carriers | 7 | 13 |
| 757 | 26 | 38 | 1669 1997 HUMAN MUTATION 10(5):393-399 Wang YC; Lin ML; Lin SJ; Li YC; Li SY Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome | 7 | 10 |
| 758 | 7 | 34 | 1696 1997 NATURE STRUCTURAL BIOLOGY 4(9):712-716 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; et al. The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome | 7 | 46 |
| 759 | 8 | 23 | 1826 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):253-256 Fisch GS; Holden JJK; Carpenter NJ; Howard-Peebles PN; Maddalena A; et al. Age-related language characteristics of children and adolescents with fragile X syndrome | 7 | 8 |
| 760 | 20 | 34 | 1847 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):191-194 Zhong N; Ju WN; Xu WM; Ye LL; Shen Y; et al. Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians | 7 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 761 | 16 | 23 | 1887 1999 DIAGNOSTIC MOLECULAR PATHOLOGY 8(3):152-156 Tzeng CC; Cho WC; Kuo PL; Chen RM Pilot fragile X screening in normal population of Taiwan | 7 | 10 |
| 762 | 42 | 62 | 2022 2000 HUMAN MOLECULAR GENETICS 9(12):1759-1769 Crawford DC; Zhang FP; Wilson B; Warren ST; Sherman SL Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability | 7 | 11 |
| 763 | 20 | 50 | 2032 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(3):2231-2238 Weisman-Shomer P; Naot Y; Fry M Tetrahelical forms of the fragile X syndrome expanded sequence d(CGG)(n) are destabilized by two heterogeneous nuclear ribonucleoprotein-related telomeric DNA-binding proteins | 7 | 10 |
| 764 | 8 | 32 | 2076 2000 MOLECULAR BRAIN RESEARCH 75(2):337-341 Valentine G; Chakravarty S; Sarvey J; Bramham C; Herkenham M Fragile X (fmr1) mRNA expression is differentially regulated in two adult models of activity-dependent gene expression | 7 | 9 |
| 765 | 16 | 86 | 2144 2001 DEVELOPMENTAL PSYCHOBIOLOGY 39(2):107-123 Roberts JE; Boccia ML; Bailey DB; Hatton DD; Skinner M Cardiovascular indices of physiological arousal in boys with fragile X syndrome | 7 | 7 |
| 766 | 15 | 44 | 2287 2002 HUMAN BRAIN MAPPING 16(4):206-218 Rivera SM; Menon V; White CD; Glaser B; Reiss AL Functional brain activation during arithmetic processing in females with fragile X Syndrome is related to FMRI protein expression | 7 | 14 |
| 767 | 15 | 32 | 2333 2002 NEUROPSYCHOLOGIA 40(8):1343-1349 Wilding J; Cornish K; Munir F Further delineation of the executive deficit in males with fragile-X syndrome | 7 | 8 |
| 768 | 18 | 33 | 2475 2003 RNA-A PUBLICATION OF THE RNA SOCIETY 9(10):1198-1207 Ramos A; Hollingworth D; Pastore A G-quartet-dependent recognition between the FMRP RGG box and RNA | 7 | 12 |
| 769 | 0 | 9 | 26 1981 LANCET 1(8219):556-557 SOUDEK D; MCGREGOR T SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 6 | 9 |
| 770 | 1 | 30 | 38 1982 AMERICAN JOURNAL OF DISEASES OF CHILDREN 136(5):389-391 TOWNES PL FRAGILE-X SYNDROME - A JIGSAW PUZZLE WITH PICTURE EMERGING | 6 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 771 | 0 | 32 | 55 1982 CANADIAN MEDICAL ASSOCIATION JOURNAL 127(2):123-126 LARBRISSEAU A; JEAN P; MESSIER B; RICHER CL FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 6 | 9 |
| 772 | 2 | 8 | 78 1982 LANCET 1(8263):100-100 SUTHERLAND GR; JACKY PB PRENATAL-DIAGNOSIS OF FRAGILE-X CHROMOSOME | 6 | 13 |
| 773 | 0 | 36 | 113 1983 AMERICAN JOURNAL OF MENTAL DEFICIENCY 87(4):372-376 PUESCHEL SM; HAYS RM; MENDOZA T FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MINOR CONGENITAL-ANOMALIES, MACRO-ORCHIDISM, AND FRAGILE X-CHROMOSOME | 6 | 8 |
| 774 | 2 | 4 | 114 1983 ANNALES DE GENETIQUE 26(3):147-149 CALVAMERCADO MP; MAUNOURY C; RETHORE MO; LEJEUNE J FRAGILE-X AND INHIBITION OF DIHYDROFOLATE-REDUCTASE - COMPARED EFFECTS OF 2 ANTIBIOTICS - TRIMETHOPRIME AND PYRIMETHAMINE | 6 | 13 |
| 775 | 9 | 17 | 116 1983 ANNALES DE GENETIQUE 26(4):247-250 TEJADA I; BOUE J; GILGENKRANTZ S PRENATAL-DIAGNOSIS OF FRAGILE X-CHROMOSOME ON AMNIOTIC-FLUID CELLS | 6 | 9 |
| 776 | 8 | 23 | 137 1983 HUMAN GENETICS 64(1):39-41 FONATSCH C; SCHWINGER E FREQUENCY OF FRAGILE-X CHROMOSOMES, FRA(X), IN LYMPHOCYTES IN RELATION TO BLOOD-STORAGE TIME AND CULTURE TECHNIQUES | 6 | 9 |
| 777 | 0 | 1 | 151 1983 JOURNAL OF MEDICAL GENETICS 20(6):476-476 MORICPETROVIC S; LACA Z A FATHER AND DAUGHTER WITH FRAGILE X-CHROMOSOME | 6 | 7 |
| 778 | 8 | 29 | 243 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(3):463-472 MULLIGAN LM; PHILLIPS MA; FORSTERGIBSON CJ; BECKETT J; PARTINGTON MW; et al. GENETIC-MAPPING OF DNA SEGMENTS RELATIVE TO THE LOCUS FOR THE FRAGILE-X SYNDROME AT XQ27.3 | 6 | 49 |
| 779 | 2 | 28 | 247 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(6):1192-1205 NUSSBAUM RL; WALMSLEY RM; LESKO JG; AIRHART SD; LEDBETTER DH THYMIDYLATE SYNTHASE-DEFICIENT CHINESE-HAMSTER CELLS - A SELECTION SYSTEM FOR HUMAN-CHROMOSOME 18 AND EXPERIMENTAL SYSTEM FOR THE STUDY OF THYMIDYLATE SYNTHASE REGULATION AND FRAGILE-X EXPRESSION | 6 | 47 |
| 780 | 9 | 44 | 281 1985 DISEASE MARKERS 3(1):9-25 JACOBS PA; SHERMAN SL THE FRAGILE(X) - A MARKER FOR THE MARTIN-BELL SYNDROME | 6 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 781 | 5 | 11 | 323 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):171-178 SIMPSON NE DERMATOGLYPHIC INDEXES OF MALES WITH THE FRAGILE-X SYNDROME AND OF THE FEMALE HETEROZYGOTES | 6 | 10 |
| 782 | 0 | 5 | 349 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):557-562 UCHIDA IA; FREEMAN VCP; BASRUR PK THE FRAGILE-X IN CATTLE | 6 | 20 |
| 783 | 2 | 9 | 386 1986 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 28(5):624-627 GILLBERG C; WAHLSTROM J; JOHANSSON R; TORNBLOM M; ALBERTSSONWIKLAND K FOLIC-ACID AS AN ADJUNCT IN THE TREATMENT OF CHILDREN WITH THE AUTISM FRAGILE-X SYNDROME (AFRAX) | 6 | 15 |
| 784 | 1 | 3 | 503 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):1-17 NERI G; OPITZ JM; MIKKELSEN M; JACOBS PA; DAVIES K; et al. CONFERENCE REPORT - 3RD INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 6 | 15 |
| 785 | 5 | 22 | 518 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):115-121 WATSON MS; BREG WR; PAULS D; BROWN WT; CARROLL AJ; et al. ANEUPLOIDY AND THE FRAGILE-X SYNDROME | 6 | 8 |
| 786 | 3 | 4 | 521 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):165-168 BUTLER MG; ALLEN GA; SINGH DN; CARPENTER NJ; HALL BD PHOTOANTHROPOMETRIC ANALYSIS OF INDIVIDUALS WITH THE FRAGILE-X SYNDROME | 6 | 10 |
| 787 | 3 | 3 | 536 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):417-422 TOMMERUP N; LAING S; CHRISTENSEN IJ; TURNER G SCREENING FOR THE FRAGILE-X - HOW MANY CELLS SHOULD WE ANALYZE | 6 | 8 |
| 788 | 3 | 4 | 547 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):625-631 SHERMAN SL; TURNER G; SHEFFIELD L; LAING S; ROBINSON H INVESTIGATION OF THE TWINNING RATE IN FAMILIES WITH THE FRAGILE-X SYNDROME | 6 | 8 |
| 789 | 4 | 9 | 633 1989 BRITISH HEART JOURNAL 61(3):289-291 SREERAM N; WREN C; BHATE M; ROBERTSON P; HUNTER S CARDIAC ABNORMALITIES IN THE FRAGILE X-SYNDROME | 6 | 9 |
| 790 | 7 | 34 | 739 1990 YALE JOURNAL OF BIOLOGY AND MEDICINE 63(4):293-299 BREGMAN JD; LECKMAN JF; ORT SI THYROID-FUNCTION IN FRAGILE-X SYNDROME MALES | 6 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 791 | 9 | 24 | 869 1991 HUMAN GENETICS 87(4):421-424 WOHRLE D; STEINBACH P FRAGILE-X EXPRESSION AND X-INACTIVATION .2. THE FRAGILE SITE AT XQ27.3 HAS A BASIC FUNCTION IN THE PATHOGENESIS OF FRAGILE X-LINKED MENTAL-RETARDATION | 6 | 8 |
| 792 | 4 | 4 | 874 1991 JOURNAL OF MEDICAL GENETICS 28(5):358-358 WEBB T; BUNDEY S PREVALENCE OF FRAGILE X-SYNDROME | 6 | 8 |
| 793 | 0 | 0 | 875 1991 JOURNAL OF MEDICAL GENETICS 28(12):809-810 JACOBS PA THE FRAGILE-X SYNDROME | 6 | 10 |
| 794 | 10 | 18 | 918 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):56-60 EINFELD S; HALL W BEHAVIOR PHENOTYPE OF THE FRAGILE X SYNDROME | 6 | 12 |
| 795 | 0 | 3 | 926 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):116-119 STEYAERT J; BORGHGRAEF M; GAULTHIER C; FRYNS JP; VANDENBERGHE H COGNITIVE PROFILE IN ADULT, NORMAL INTELLIGENT FEMALE FRAGILE-X CARRIERS | 6 | 9 |
| 796 | 38 | 84 | 1106 1993 GENETIC COUNSELING 4(4):245-263 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H FRAGILE-X SYNDROME AND AUTISM - A PREVALENT ASSOCIATION OR A MISINTERPRETED CONNECTION | 6 | 13 |
| 797 | 1 | 1 | 1158 1993 NATURE GENETICS 5(3):312-312 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; et al. TISSUE-SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE X-SYNDROME (VOL 3, PG 36, 1993) | 6 | 7 |
| 798 | 3 | 12 | 1160 1993 NEUROPEDIATRICS 24(4):211-213 REES M; DIEBOLD U; PARKER K; DOOSE H; GARDINER RM; et al. BENIGN CHILDHOOD EPILEPSY WITH CENTROTEMPORAL SPIKES AND THE FOCAL SHARP WAVE TRAIT IS NOT LINKED TO THE FRAGILE-X REGION | 6 | 23 |
| 799 | 11 | 27 | 1166 1993 SOMATIC CELL AND MOLECULAR GENETICS 19(4):393-404 LUO SY; ROBINSON JC; REISS AL; MIGEON BR DNA METHYLATION OF THE FRAGILE-X LOCUS IN SOMATIC AND GERM-CELLS DURING FETAL DEVELOPMENT - RELEVANCE TO THE FRAGILE-X SYNDROME AND X-INACTIVATION | 6 | 19 |
| 800 | 16 | 27 | 1257 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:27-35 SABARATNAM M; LAVER S; BUTLER L; PEMBREY M FRAGILE-X SYNDROME IN NORTH-EAST ESSEX - TOWARDS SYSTEMATIC SCREENING - CLINICAL-SELECTION | 6 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 801 | 12 | 24 | 1333 1995 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 172(4):1236-1239 RYYNANEN M; KIRKINEN P; MANNERMAA A; SAARIKOSKI S CARRIER DIAGNOSIS OF THE FRAGILE-X SYNDROME - A CHALLENGE IN ANTENATAL CLINICS | 6 | 8 |
| 802 | 7 | 8 | 1379 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):405-407 Holden JJA; Chalifoux M; Wing M; JulienInalsingh C; Lawson JS; et al. Distribution and frequency of FMR1 CGG repeat numbers in the general population | 6 | 13 |
| 803 | 20 | 28 | 1395 1995 HUMAN GENETICS 96(5):577-584 ELALEEM AA; BOHM I; TEMTAMY S; ELAWADY M; AWADALLA M; et al. DIRECT MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME IN A SAMPLE OF EGYPTIAN AND GERMAN PATIENTS USING NONRADIOACTIVE PCR AND SOUTHERN BLOT FOLLOWED BY CHEMILUMINESCENT DETECTION | 6 | 9 |
| 804 | 16 | 40 | 1417 1995 JOURNAL OF MEDICAL GENETICS 32(10):764-769 DEVRIES BBA; ROBINSON H; STOLTEDIJKSTRA I; GI CVTP; DIJKSTRA PF; et al. GENERAL OVERGROWTH IN THE FRAGILE-X SYNDROME - VARIABILITY IN THE PHENOTYPIC-EXPRESSION OF THE FMR1 GENE MUTATION | 6 | 16 |
| 805 | 11 | 34 | 1430 1995 NUCLEIC ACIDS RESEARCH 23(11):1876-1881 MITCHELL JE; NEWBURY SF; MCCLELLAN JA COMPACT STRUCTURES OF D(CNG)(N) OLIGONUCLEOTIDES IN SOLUTION AND THEIR POSSIBLE RELEVANCE TO FRAGILE-X AND RELATED HUMAN GENETIC-DISEASES | 6 | 31 |
| 806 | 11 | 12 | 1457 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):176-180 Perroni L; Grasso M; Argusti A; LoNigro C; Croci GF; et al. Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families | 6 | 7 |
| 807 | 12 | 31 | 1482 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):323-328 Mazzocco MMM; Holden JJA Neuropsychological profiles of three sisters homozygous for the fragile X premutation | 6 | 8 |
| 808 | 11 | 28 | 1501 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 67(1):77-80 Simon EW; Finucane BM Facial emotion identification in males with fragile X syndrome | 6 | 6 |
| 809 | 19 | 26 | 1535 1996 HUMAN GENETICS 97(4):512-515 Mornet E; Chateau C; Taillandier A; SimonBouy B; Serre JL Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndrome | 6 | 8 |
| 810 | 21 | 29 | 1542 1996 HUMAN MOLECULAR GENETICS 5(6):821-825 Mornet E; Chateau C; Hirst MC; Thepot F; Taillandier A; et al. Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline range | 6 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 811 | 12 | 14 | 1567 1996 PEDIATRIC NEUROLOGY 15(4):358-360 Kluger G; Bohm I; Laub MC; Waldenmaier C Epilepsy and fragile X gene mutations | 6 | 12 |
| 812 | 6 | 10 | 1633 1997 ANNALS OF CLINICAL BIOCHEMISTRY 34:517-520 Chen TA; Lu XF; Che PK; Ho WKK Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects | 6 | 7 |
| 813 | 32 | 57 | 1675 1997 JOURNAL OF INHERITED METABOLIC DISEASE 20(2):139-151 Hoogeveen AT; Oostra BA The fragile X syndrome | 6 | 10 |
| 814 | 76 | 123 | 1710 1997 WESTERN JOURNAL OF MEDICINE 166(2):129-137 Hagerman RJ Fragile X syndrome - Molecular and clinical insights and treatment issues | 6 | 8 |
| 815 | 24 | 39 | 1713 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 75(3):277-282 Jara L; Aspillaga M; Avendano I; Obreque V; Blanco R; et al. Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population | 6 | 7 |
| 816 | 24 | 41 | 1773 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:81-89 Elbaz A; Suedois J; Duquesnoy M; Beldjord C; Berchel C; et al. Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies | 6 | 8 |
| 817 | 3 | 6 | 1868 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(5):436-439 Einfeld S; Tonge B; Turner G Longitudinal course of behavioral and emotional problems in Fragile X syndrome | 6 | 6 |
| 818 | 10 | 14 | 1972 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):105-107 Tuncbilek E; Alikasifoglu M; Aktas D; Duman F; Yanik H; et al. Screening for the fragile X syndrome among mentally retarded males by hair root analysis | 6 | 6 |
| 819 | 32 | 45 | 2085 2000 NUCLEIC ACIDS RESEARCH 28(7):1535-1541 Weisman-Shomer P; Cohen E; Fry M Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures | 6 | 11 |
| 820 | 23 | 55 | 2123 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(3):216-230 Roberts JE; Mirrett P; Burchinal M Receptive and expressive communication development of young males with fragile X syndrome | 6 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 821 | 45 | 85 | 2132 2001 BRAIN RESEARCH BULLETIN 56(3-4):375-382 Bardoni B; Schenck A; Mandel JL The Fragile X mental retardation protein | 6 | 9 |
| 822 | 16 | 17 | 2136 2001 CELL 107(5):555-557 Kaytor MD; Orr HT RNA targets of the fragile X protein | 6 | 15 |
| 823 | 19 | 31 | 2162 2001 INFANTS AND YOUNG CHILDREN 14(1):24-33 Bailey DB; Roberts JE; Mirrett P; Hatton DD Identifying infants and toddlers with fragile X syndrome: Issues and recommendations | 6 | 6 |
| 824 | 18 | 62 | 2236 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 108(2):105-116 Hatton DD; Hooper SR; Bailey DB; Skinner ML; Sullivan KM; et al. Problem behavior in boys with fragile X syndrome | 6 | 7 |
| 825 | 12 | 24 | 2251 2002 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 292(4):1063-1069 Denman RB; Sung YJ Species-specific and isoform-specific RNA binding of human and mouse fragile X mental retardation proteins | 6 | 6 |
| 826 | 8 | 61 | 2297 2002 JOURNAL OF COGNITIVE NEUROSCIENCE 14(2):160-171 Tamm L; Menon V; Johnston CK; Hessl DR; Reiss AL fMRI study of cognitive interference processing in females with fragile X syndrome | 6 | 10 |
| 827 | 32 | 51 | 2298 2002 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 23(6):416-423 Loesch DZ; Huggins RM; Bui QM; Epstein JL; Taylor AK; et al. Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile X males and females assessed by robust pedigree analysis | 6 | 6 |
| 828 | 13 | 25 | 2305 2002 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 41(3):237-244 Dyer-Friedman J; Glaser B; Hessl D; Johnston C; Huffman LC; et al. Genetic and environmental influences on the cognitive outcomes of children with fragile X syndrome | 6 | 6 |
| 829 | 9 | 20 | 2331 2002 NEURON 34(6):859-862 Gao FB Understanding fragile X syndrome: Insights from retarded flies | 6 | 8 |
| 830 | 19 | 43 | 2343 2002 PSYCHONEUROENDOCRINOLOGY 27(7):855-872 Hessl D; Glaser B; Dyer-Friedman J; Blasey C; Hastie T; et al. Cortisol and behavior in fragile X syndrome | 6 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 831 | 13 | 15 | 2347 2002 TRENDS IN MOLECULAR MEDICINE 8(3):102-103 Oostra BA Functions of the fragile X protein | 6 | 8 |
| 832 | 27 | 40 | 2399 2003 BIOCHEMISTRY 42(35):10437-10444 Adinolfi S; Ramos A; Martin SR; Dal Piaz F; Pucci P; et al. The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding | 6 | 7 |
| 833 | 28 | 61 | 2420 2003 EXPERIMENTAL CELL RESEARCH 289(1):95-107 Bardoni B; Willemsen R; Weiler IJ; Schenck A; Severijnen LA; et al. NUFIP 1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosome | 6 | 7 |
| 834 | 22 | 55 | 2531 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(4):460-469 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; et al. Penetrance of the fragile X - Associated tremor/ataxia syndrome in a premutation carrier population | 6 | 15 |
| 835 | 40 | 97 | 2560 2004 JOURNAL OF NEUROSCIENCE 24(25):5798-5809 Michel CI; Kraft R; Restifo LL Defective neuronal development in the mushroom bodies of Drosophila Fragile X Mental Retardation 1 Mutants | 6 | 7 |
| 836 | 26 | 61 | 2610 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(36):13357-13362 Khandjian EW; Huot ME; Tremblay S; Davidovic L; Mazroui R; et al. Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles | 6 | 7 |
| 837 | 1 | 15 | 37 1981 PEDIATRICS 68(4):594-595 GERALD PS X-LINKED MENTAL-RETARDATION AND THE FRAGILE-X SYNDROME | 5 | 11 |
| 838 | 0 | 0 | 44 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A110-A110 SHAPIRO LR; HASEN J; GORDON G; SOUTHREN AL; WILMOT PL; et al. TESTICULAR INSUFFICIENCY AND DISORDERED THYROID METABOLISM IN THE FRAGILE X-CHROMOSOME SYNDROME | 5 | 7 |
| 839 | 0 | 5 | 62 1982 HUMAN GENETICS 60(1):80-81 ZANKL H; EBERLE G METHODS OF INCREASING THE VISIBILITY OF FRAGILE-X CHROMOSOMES | 5 | 8 |
| 840 | 2 | 13 | 107 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):1270-1275 MIXON JC; DEV VG FRAGILE-X EXPRESSION IS DECREASED BY 5-AZACYTIDINE AND S-ADENOSYLHOMOCYSTEINE | 5 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 841 | 0 | 4 | 154 1983 LANCET 2(8364):1427-1427 KINNELL HG; BANU SP INSTITUTIONAL PREVALENCE OF FRAGILE X-SYNDROME | 5 | 8 |
| 842 | 6 | 36 | 191 1984 AMERICAN JOURNAL OF MEDICINE 77(4):602-611 BRANDA RF; ARTHUR DC; WOODS WG; DANZL TJ; KING RA FOLATE METABOLISM AND CHROMOSOMAL STABILITY IN THE FRAGILE-X SYNDROME | 5 | 14 |
| 843 | 1 | 9 | 195 1984 CLINICAL GENETICS 25(2):135-139 GARDINER GB; WENGER SL; STEELE MW INVITRO REVERSAL OF FRAGILE-X EXPRESSION BY EXOGENOUS THYMIDINE | 5 | 7 |
| 844 | 6 | 16 | 234 1984 PRENATAL DIAGNOSIS 4(1):61-66 WILSON MG; MARCHESE CA PRENATAL-DIAGNOSIS OF FRAGILE-X IN A HETEROZYGOUS FEMALE FETUS AND POSTNATAL FOLLOW-UP | 5 | 9 |
| 845 | 3 | 19 | 257 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):771-772 TRUSLER S; BEATTYDESANA J FRAGILE X-SYNDROME - A PUBLIC-HEALTH CONCERN | 5 | 6 |
| 846 | 4 | 8 | 267 1985 CLINICAL GENETICS 27(5):520-521 WEBB GC DETECTION OF THE FRAGILE X-CHROMOSOME AND OTHER FRAGILE SITES | 5 | 6 |
| 847 | 13 | 28 | 287 1985 HUMAN GENETICS 69(3):218-223 VONKOSKULL H; AULA P; AMMALA P; NORDSTROM AM; RAPOLA J IMPROVED TECHNIQUE FOR THE EXPRESSION OF FRAGILE-X IN CULTURED AMNIOTIC-FLUID CELLS | 5 | 9 |
| 848 | 2 | 7 | 311 1985 PRENATAL DIAGNOSIS 5(3):229-231 ROCCHI M; PECILE V; ARCHIDIACONO N; MONNI G; DUMEZ Y; et al. PRENATAL-DIAGNOSIS OF THE FRAGILE-X IN MALE MONOZYGOTIC TWINS - DISCORDANT EXPRESSION OF THE FRAGILE SITE IN AMNIOCYTES | 5 | 10 |
| 849 | 1 | 14 | 342 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):445-455 LEDBETTER DH; AIRHART SD; NUSSBAUM RL CAFFEINE ENHANCES FRAGILE-(X) EXPRESSION IN SOMATIC-CELL HYBRIDS | 5 | 18 |
| 850 | 8 | 16 | 343 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):467-473 KRAWCZUN MS; LELE KP; JENKINS EC; BROWN WT FRAGILE-X EXPRESSION INCREASED BY LOW CELL-CULTURE DENSITY | 5 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 851 | 8 | 18 | 394 1986 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 7(4):253-256 MADISON LS; WELLS TE; FRISTO TE; BENESCH CG A CONTROLLED-STUDY OF FOLIC-ACID TREATMENT IN 3 FRAGILE-X SYNDROME MALES | 5 | 6 |
| 852 | 8 | 19 | 418 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):909-914 WENGER SL; HENNESSEY JC; STEELE MW INCREASED SISTER CHROMATID EXCHANGE FREQUENCY AT XQ27-SITE IN AFFECTED FRAGILE-X MALES | 5 | 23 |
| 853 | 7 | 17 | 423 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 28(1):13-15 CHUDLEY AE; DEVONFLINDT R; HAGERMAN RJ COGNITIVE VARIABILITY IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 854 | 13 | 30 | 428 1987 ARCHIVES OF OPHTHALMOLOGY 105(8):1099-1102 STORM RL; PEBENITO R; FERRETTI C OPHTHALMOLOGIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 7 |
| 855 | 6 | 34 | 433 1987 BIOLOGICAL PSYCHIATRY 22(3):303-312 STCLAIR DM; BLACKWOOD DHR; OLIVER CJ; DICKENS P P3 ABNORMALITY IN FRAGILE-X SYNDROME | 5 | 16 |
| 856 | 2 | 4 | 434 1987 BRITISH JOURNAL OF PSYCHIATRY 150:700-702 DEB S; COWIE VA; TIMBERLAKE C A CASE OF MOSAICISM WITH FRAGILE-X AND FRAGILE-XXY COMPONENTS | 5 | 5 |
| 857 | 4 | 7 | 495 1987 PRENATAL DIAGNOSIS 7(3):197-202 SUTHERLAND GR; BAKER E; PURVISSMITH S; HOCKEY A; KRUMINS E; et al. PRENATAL-DIAGNOSIS OF THE FRAGILE-X USING THYMIDINE INDUCTION | 5 | 13 |
| 858 | 8 | 20 | 515 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):83-98 WALDSTEIN G; HAGERMAN R AORTIC HYPOPLASIA AND CARDIAC VALVULAR ABNORMALITIES IN A BOY WITH FRAGILE-X SYNDROME | 5 | 5 |
| 859 | 4 | 5 | 548 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):633-639 SHERMAN SL; TURNER G; ROBINSON H; LAING S INVESTIGATION OF THE SEGREGATION OF THE FRAGILE-X MUTATION IN DAUGHTERS OF OBLIGATE CARRIER WOMEN | 5 | 7 |
| 860 | 7 | 21 | 553 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):681-688 WARREN ST FRAGILE-X SYNDROME - A HYPOTHESIS REGARDING THE MOLECULAR MECHANISM OF THE PHENOTYPE | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 861 | 4 | 44 | 570 1988 BRAIN AND LANGUAGE 34(2):203-221 VILKMAN E; NIEMI J; IKONEN U FRAGILE-X SPEECH PHONOLOGY IN FINNISH | 5 | 6 |
| 862 | 1 | 13 | 575 1988 CLINICAL GENETICS 33(5):349-355 MERYASH DL; ABUELO D COUNSELING NEEDS AND ATTITUDES TOWARD PRENATAL-DIAGNOSIS AND ABORTION IN FRAGILE-X FAMILIES | 5 | 17 |
| 863 | 19 | 43 | 683 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 35(1):22-27 MINGRONINETTO RC; ROSENBERG C; VIANNAMORGANTE AM; PAVANELLO RDM FRAGILE-X FREQUENCY IN A MENTALLY-RETARDED POPULATION IN BRAZIL | 5 | 8 |
| 864 | 9 | 32 | 691 1990 AMERICAN JOURNAL ON MENTAL RETARDATION 94(4):442-447 CANTU ES; STONE JW; WING AA; LANGEE HR; WILLIAMS CA CYTOGENETIC SURVEY FOR AUTISTIC FRAGILE-X CARRIERS IN A MENTAL-RETARDATION CENTER | 5 | 16 |
| 865 | 3 | 10 | 727 1990 NEUROLOGY 40(2):378-380 DESAI HB; DONAT J; SHOKEIR MHK; MUNOZ DG AMYOTROPHIC LATERAL SCLEROSIS IN A PATIENT WITH FRAGILE X-SYNDROME | 5 | 7 |
| 866 | 4 | 11 | 822 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):453-455 SHAPIRO LR; WILMOT PL; MURPHY PD PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - POSSIBLE END OF THE EXPERIMENTAL PHASE FOR AMNIOTIC-FLUID | 5 | 6 |
| 867 | 5 | 15 | 833 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 39(3):374-375 MOORE PSJ; CHUDLEY AE; WINTER JSD PITUITARY-GONADAL AXIS IN PREPUBERTAL BOYS WITH THE FRAGILE-X SYNDROME | 5 | 7 |
| 868 | 2 | 12 | 837 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 41(3):275-278 LACHIEWICZ AM; HOEGERMAN SF; HOLMGREN G; HOLMBERG E; ARINBJARNARSON K ASSOCIATION OF THE ROBIN SEQUENCE WITH THE FRAGILE-X SYNDROME | 5 | 8 |
| 869 | 6 | 28 | 872 1991 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 21(4):503-516 HODAPP RM; DYKENS EM; ORT SI; ZELINSKY DG; LECKMAN JF CHANGING PATTERNS OF INTELLECTUAL STRENGTHS AND WEAKNESSES IN MALES WITH FRAGILE-X SYNDROME | 5 | 16 |
| 870 | 9 | 18 | 884 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):831-834 HILTON DK; MARTIN CA; HEFFRON WM; HALL BD; JOHNSON GL IMIPRAMINE TREATMENT OF ADHD IN A FRAGILE-X CHILD | 5 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 871 | 0 | 0 | 898 1991 OPTOMETRY AND VISION SCIENCE 68(8):634-640 MAINO DM; WESSON M; SCHLANGE D; CIBIS G; MAINO JH OPTOMETRIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 872 | 24 | 31 | 914 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):5-27 MANDEL JL; HAGERMAN R; FROSTER U; BROWN WT; JENKINS EC; et al. 5TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 5 | 8 |
| 873 | 15 | 23 | 923 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):87-95 HINTON VJ; DOBKIN CS; HALPERIN JM; JENKINS EC; BROWN WT; et al. MODE OF INHERITANCE INFLUENCES BEHAVIORAL EXPRESSION AND MOLECULAR CONTROL OF COGNITIVE DEFICITS IN FEMALE CARRIERS OF THE FRAGILE-X SYNDROME | 5 | 8 |
| 874 | 9 | 13 | 939 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):192-196 VERKERK AJMH; DEVRIES BBA; NIERMEIJER MF; FU YH; NELSON DL; et al. INTRAGENIC PROBE USED FOR DIAGNOSTICS IN FRAGILE-X FAMILIES | 5 | 6 |
| 875 | 4 | 9 | 1079 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 47(2):216-220 WIEGERS AM; CURFS LMG; VERMEER ELMH; FRYNS JP ADAPTIVE-BEHAVIOR IN THE FRAGILE X-SYNDROME - PROFILE AND DEVELOPMENT | 5 | 6 |
| 876 | 14 | 31 | 1109 1993 HUMAN GENETICS 91(5):469-474 LOESCH DZ; SHEFFIELD LJ; HAY DA BETWEEN-GENERATION DIFFERENCES IN ASCERTAINMENT AND PENETRANCE - RELEVANCE TO GENETIC HYPOTHESES IN FRAGILE-X | 5 | 5 |
| 877 | 6 | 13 | 1162 1993 PEDIATRICS 91(4):714-715 CRABBE LS; BENSKY AS; HORNSTEIN L; SCHWARTZ DC CARDIOVASCULAR-ABNORMALITIES IN CHILDREN WITH FRAGILE-X SYNDROME | 5 | 7 |
| 878 | 15 | 19 | 1199 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):458-462 TURNER AM; ROBINSON H; WAKE S; LAING SJ; LEIGH D; et al. COUNSELING RISK FIGURES FOR FRAGILE-X CARRIER FEMALES OF VARYING BAND SIZES FOR USE IN PREDICTING THE LIKELIHOOD OF RETARDATION IN THEIR OFFSPRING | 5 | 8 |
| 879 | 0 | 3 | 1217 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):382-382 HOWARDPEEBLES PN; MADDALENA A; SPENCE WC; LEVINSON G; FALLON L; et al. FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 5 | 9 |
| 880 | 23 | 37 | 1408 1995 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 17(4):518-528 HINTON VJ; HALPERIN JM; DOBKIN CS; DING XH; BROWN WT; et al. COGNITIVE AND MOLECULAR ASPECTS OF FRAGILE-X | 5 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 881 | 17 | 27 | 1416 1995 JOURNAL OF MEDICAL GENETICS 32(3):236-239 MACPHERSON JN; CURTIS G; CROLLA JA; DENNIS N; MIGEON B; et al. UNUSUAL (CGG)(N) EXPANSION AND RECOMBINATION IN A FAMILY WITH FRAGILE-X AND DIGEORGE-SYNDROME | 5 | 11 |
| 882 | 14 | 35 | 1419 1995 JOURNAL OF MEDICAL GENETICS 32(12):925-929 KIRCHGESSNER CU; WARREN ST; WILLARD HF X INACTIVATION OF THE FMR1 FRAGILE-X MENTAL-RETARDATION GENE | 5 | 13 |
| 883 | 27 | 61 | 1427 1995 NEUROPSYCHOLOGY 9(4):470-480 MAZZOCCO MMM; FREUND LS; BAUMGARDNER TL; FORMAN L; REISS AL NEUROPSYCHOLOGICAL AND PSYCHOSOCIAL EFFECTS OF THE FMR-1 FULL MUTATION - CASE-REPORT OF MONOZYGOTIC TWINS DISCORDANT FOR THE FRAGILE-X SYNDROME | 5 | 6 |
| 884 | 18 | 37 | 1444 1996 AMERICAN JOURNAL OF HUMAN GENETICS 59(3):540-546 Vaisanen ML; Haataja R; Leisti L Decrease in the CGG(n) trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission | 5 | 9 |
| 885 | 13 | 17 | 1473 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):270-273 MingroniNetto RC; Haddad LA; ViannaMorgante AM The number of CGG repeats of the FMR1 locus in premutated and fully mutated heterozygotes and their offspring: Implications for the origin of mosaicism | 5 | 6 |
| 886 | 4 | 9 | 1481 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):319-322 Fisch GS; Carpenter N; Maddalena A; Tarleton J; JulienInalsingh C; et al. Rater reliability of fragile X mutation size estimates: A multilaboratory analysis | 5 | 5 |
| 887 | 20 | 27 | 1528 1996 EUROPEAN JOURNAL OF HUMAN GENETICS 4(1):8-12 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; et al. Unexpected inheritance of the (CGG)(n) trinucleotide expansion in a fragile X syndrome family | 5 | 6 |
| 888 | 58 | 71 | 1530 1996 EUROPEAN PSYCHIATRY 11(5):233-243 Franke P; Barbe B; Leboyer M; Maier W Fragile X syndrome .2. Cognitive and behavioral correlates of mutations of the FMR-1 gene | 5 | 6 |
| 889 | 14 | 34 | 1538 1996 HUMAN GENETICS 98(4):409-414 Schmucker B; Ballhausen WG; Pfeiffer RA Mosaicism of a microdeletion of 486 bp involving the CGG repeat of the FMR1 gene due to misalignment of GTT tandem repeats at chi-like elements flanking both breakpoints and a full mutation | 5 | 12 |
| 890 | 11 | 50 | 1548 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(40):24325-24328 Godde JS; Kass SU; Hirst MC; Wolffe AP Nucleosome assembly on methylated CGG triplet repeats in the Fragile X Mental Retardation gene 1 promoter | 5 | 41 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 891 | 28 | 44 | 1619 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):961-967 Gronskov K; Hjalgrim H; Bjerager MO; BrondumNielsen K Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression | 5 | 6 |
| 892 | 3 | 11 | 1623 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 69(1):114-116 Martin NG; Healey SC; Pangan TS; Heath AC; Turner G Do mothers of dizygotic twins have earlier menopause? A role for fragile X? | 5 | 12 |
| 893 | 8 | 10 | 1643 1997 BRITISH MEDICAL JOURNAL 315(7117):1223-1226 Turner G; Robinson H; Wake S; Laing S; Partington M Case finding for the fragile X syndrome and its consequences | 5 | 9 |
| 894 | 8 | 11 | 1660 1997 HUMAN GENETICS 99(6):793-795 Chen SH; Schoof JM; Buroker NE; Scott CR The identification of a (CGG)(6)AGG insertion within the CGG repeat of the FMR1 gene in Asians | 5 | 6 |
| 895 | 15 | 47 | 1672 1997 JOURNAL OF BIOLOGICAL CHEMISTRY 272(27):16761-16768 Deissler H; Wilm M; Genc B; Schmitz B; Ternes T; et al. Rapid protein sequencing by tandem mass spectrometry and cDNA cloning of p20-CGGBP - A novel protein that binds to the unstable triplet repeat 5'-d(CGG)(n)-3' in the human FMR1 gene | 5 | 17 |
| 896 | 0 | 5 | 1823 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(2):140-141 Hjalgrim H; Jacobsen TB; Norgaard K; Lou HC; Brondum-Nielsen K; et al. Frontal-subcortical hypofunction in the fragile X syndrome | 5 | 8 |
| 897 | 22 | 25 | 1853 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):221-225 Schmucker B; Seidel J Mosaicism for a full mutation and a normal size allele in two fragile X males | 5 | 7 |
| 898 | 10 | 20 | 1854 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):226-228 Glaser D; Wohrle D; Salat U; Vogel W; Steinbach P; et al. Mitotic behavior of expanded CGG repeats studied on cultured cells: Further evidence for methylation-mediated triplet repeat stability in fragile X syndrome | 5 | 8 |
| 899 | 12 | 20 | 2075 2000 MOLECULAR AND CELLULAR PROBES 14(2):115-119 Mila M; Castellvi-Bel S; Sanchez A; Barcelo A; Badenas C; et al. Rare variants in the promoter of the fragile X syndrome gene (FMR1) | 5 | 5 |
| 900 | 16 | 58 | 2124 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(5):389-400 Sudhalter V; Belser RC Conversational characteristics of children with fragile x syndrome: Tangential language | 5 | 8 |